Azithromycin

Product NDC

0093-7147

11-digit product format

000937147

Labeler code

0093

Product ID

0093-7147_6bb55b3a-1790-426e-9a68-f5fd0f0d4d62

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Azithromycin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA065150

Marketing category

ANDA

Marketing start

2005-11-16

Marketing end

0000-00-00

Substance

AZITHROMYCIN MONOHYDRATE

Active strength

600 mg/1

Pharmacologic classes

Macrolide Antimicrobial [EPC],Macrolides [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record